Matsushita T, Amagai Y, Soga T, Terai K, Obinata M, Hashimoto S
Molecular Medicine Laboratories Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Co., Ltd., 21 Miyukigaoka, Tsukuba-shi, Ibaraki, 305-8585 Japan.
Neuroscience. 2005;136(1):115-21. doi: 10.1016/j.neuroscience.2005.07.011. Epub 2005 Sep 21.
The successive stages of development from oligodendrocyte progenitor to mature oligodendrocyte have been investigated in detail by using stage-specific antibodies. However, no cell lines are available that show stepwise differentiation from oligodendrocyte progenitors to mature oligodendrocytes. Here we show the establishment of an immortalized oligodendrocyte cell line, OLP6, from adult transgenic rats harboring the temperature-sensitive simian virus 40 large T-antigen gene. The OLP6 cells had a fibroblastic morphology and continuously proliferated at 33 degrees C. They displayed growth arrest and multipolar morphology when they were cultured at 39 degrees C. They express the oligodendrocytic markers O4, 2'-3'-cyclic-nucleotide 3'-phosphodiesterase, galactocerebroside and second endothelial differentiation gene receptor-2 at 39 degrees C. The OLP6 cells underwent apoptosis upon serum withdrawal at 39 degrees C. Lysophosphatidic acid inhibited this apoptosis and promoted the expression of myelin basic protein. These results demonstrate that the activation of endothelial differentiation gene receptor-2 exerts anti-apoptosis and myelinogenesis effects on the OLP6 cells. Taken together, the OLP6 cells in the late oligodendrocyte progenitor stage can progress to the immature oligodendrocyte stage by shifting culture temperature. Furthermore, lysophosphatidic acid promoted the maturation of OLP6 cells in the immature oligodendrocyte stage. Such OLP6 cells should provide a potent model system for studying the precise mechanism involved in stepwise differentiation of oligodendrocytes.
利用阶段特异性抗体,已对少突胶质细胞前体细胞到成熟少突胶质细胞的连续发育阶段进行了详细研究。然而,目前尚无能够显示从少突胶质细胞前体细胞逐步分化为成熟少突胶质细胞的细胞系。在此,我们展示了一种永生化少突胶质细胞系OLP6的建立,该细胞系源自携带温度敏感型猿猴病毒40大T抗原基因的成年转基因大鼠。OLP6细胞具有成纤维细胞形态,在33℃时持续增殖。当在39℃培养时,它们表现出生长停滞和多极形态。在39℃时,它们表达少突胶质细胞标志物O4、2'-3'-环核苷酸3'-磷酸二酯酶、半乳糖脑苷脂和第二代内皮分化基因受体-2。在39℃血清撤出后,OLP6细胞发生凋亡。溶血磷脂酸抑制这种凋亡并促进髓鞘碱性蛋白的表达。这些结果表明,内皮分化基因受体-2的激活对OLP6细胞发挥抗凋亡和髓鞘形成作用。综上所述,处于少突胶质细胞前体晚期阶段的OLP6细胞可通过改变培养温度进展到未成熟少突胶质细胞阶段。此外,溶血磷脂酸促进了处于未成熟少突胶质细胞阶段的OLP6细胞的成熟。这样的OLP6细胞应为研究少突胶质细胞逐步分化所涉及的精确机制提供一个有力的模型系统。